Tournicare Pty, Ltd.
AustraliaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tournicare Pty, Ltd. have in the registry?
The registry currently lists 1 device for Tournicare Pty, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tournicare Pty, Ltd.'s devices?
Among its 1 most recently registered device, Tournicare Pty, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Tournicare Pty, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tournicare Pty, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tournicare Pty, Ltd. in the registry?
The most recently registered devices listed for Tournicare Pty, Ltd. include Tournicare ARMA Automatic Blood Pressure Monitor (ARMA-08).